Результаты поиска - Sandra Nagl

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  1. 1
    Underwater vs Conventional Endoscopic Mucosal Resection of Large Sessile or Flat Colorectal Polyps: A Prospective Randomized Controlled Trial

    Underwater vs Conventional Endoscopic Mucosal Resection of Large Sessile or Flat Colorectal Polyps: A Prospective Randomized Controlled Trial по Sandra Nagl, Alanna Ebigbo, Stefan Goelder, Christoph Roemmele, Lukas Neuhaus, Tobias Weber, Georg Braun, Andreas Probst, Elisabeth Schnoy, Agnieszka Kafel, Anna Muzalyova, Helmut Messmann

    Опубликовано 2021
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    Artigo
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  2. 2
    A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

    A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes по Marwan Shinawi, Christian P. Schaaf, Samarth Bhatt, Zhilian Xia, Ankita Patel, Sau Wai Cheung, Brendan C. Lanpher, Sandra Nagl, Heinrich Stephan Herding, Claudia Nevinny-Stickel, LaDonna Immken, Gayle Patel, Jennifer R. German, Arthur L. Beaudet, Paweł Stankiewicz

    Опубликовано 2009
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    Artigo
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  3. 3
    Influence of artificial intelligence on the diagnostic performance of endoscopists in the assessment of Barrett’s esophagus: a tandem randomized and video trial

    Influence of artificial intelligence on the diagnostic performance of endoscopists in the assessment of Barrett’s esophagus: a tandem randomized and video trial по M. Meinikheim, Robert Mendel, Christoph Palm, Andreas Probst, Anna Muzalyova, M. W. Scheppach, Sandra Nagl, Elisabeth Schnoy, Christoph Römmele, Dominik Schulz, J. Schlottmann, Friederike Prinz, David Rauber, T. Rückert, Tomoaki Matsumura, Glòria Fernández–Esparrach, Nasim Parsa, Michael F. Byrne, Helmut Messmann, Alanna Ebigbo

    Опубликовано 2024
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    Artigo
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  4. 4
    Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

    Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 по Anne Gregor, Beate Albrecht, Ingrid Bader, Emilia K. Bijlsma, Arif B. Ekici, Hartmut Engels, Karl Hackmann, Denise Horn, Juliane Hoyer, Jakub Klapecki, Jürgen Kohlhase, Isabelle Maystadt, Sandra Nagl, Eva Christina Prott, Sigrid Tinschert, Reinhard Ullmann, Eva Wohlleber, Geoffrey Woods, André Reis, Anita Rauch, Christiane Zweier

    Опубликовано 2011
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    Artigo
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  5. 5
    Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and<i>PEX26</i>mutated in Heimler syndrome

    Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read... по Christine Neuhaus, Tobias Eisenberger, Christian Decker, Sandra Nagl, Cornelia Blank, Markus Pfister, Ingo Kennerknecht, Cornelie Müller-Hofstede, Peter Charbel Issa, Raoul Heller, Bodo B. Beck, Klaus Rüther, Diana Mitter, Klaus Rohrschneider, Ute Steinhauer, Heike Korbmacher, Dagmar Huhle, Solaf M. Elsayed, Hesham M. Taha, Shahid Mahmood Baig, Heidi Stöhr, Markus N. Preising, Susanne Markus, Fabian Moeller, Birgit Lorenz, Kerstin Nagel‐Wolfrum, Arif O. Khan, Hanno J. Bolz

    Опубликовано 2017
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    Artigo
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